Canonical Allele Identifier: CA388972034
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375669-C-T
MyVariant Identifiers: chr14:g.23844878C>T (hg19) chr14:g.23375669C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375669C>T , CM000676.2:g.23375669C>T GRCh38
NC_000014.8:g.23844878C>T , CM000676.1:g.23844878C>T GRCh37
NC_000014.7:g.22914718C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.275C>T MANE Select ENSP00000380417.2:p.Ala92Val
ENST00000329715.2:c.323C>T ENSP00000328111.2:p.Ala108Val
ENST00000397242.2:c.275C>T ENSP00000380417.2:p.Ala92Val
NM_022789.3:c.323C>T NP_073626.1:p.Ala108Val
NM_172314.1:c.275C>T NP_758525.1:p.Ala92Val
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